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Filtered Search Results
FUJIFILM Biosciences 100MG VIAL L-012 LUMINOL CHEMI
*Orders for this supplier are non-cancellable/non-returnable once they are processed.*
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AVANTI POLAR LIPIDS INC 17 0 SM D18 1 5MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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NC3404283 17 0 SM D18 1 5MG
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Medchemexpress LLC Y-27632 1Mg | HY-10071
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Y-27632 1Mg
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HPC STANDARDS US D4-BETA-DAMASCENONE 1 X 5MG
NC2940273 D4-BETA-DAMASCENONE 1 X 5MG
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Medchemexpress LLC Retatrutide, 99.96%, 10mg
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Retatrutide (LY3437943) is a triple agonist peptide of the glucagon receptor (GCGR), glucosedependent insulinotropic polypeptide receptor (GIPR), and glucagon-like peptide-1 receptor (GLP-1R). Retatrutide binds human GCGR, GIPR, and GLP-1R with EC50 values of 5.79, 0.0643 and 0.775 nM, respectively. Retatrutide can be used for the research of obesity.
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Medchemexpress LLC Tarlatamab Amg-757 1Mg | HY-P99575-1MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Tarlatamab Amg-757 1Mg
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STEMCELL Technologies Valproic Acid (Sodium Salt), Size: 500 mg
Inhibit Histone Deacetylases (HDACs) with Valproic Acid (VPA). This epigenetic modifier modulates osteogenic differentiation of human mesenchymal stem cells (Cho et al. J Cell Biochem, 2005), and together with other factors, it allows for the direct lineage reprogramming of fibroblasts to mature neurons (Hu et al. Cell Stem Cell, 2015) and the reprogramming of human fibroblasts to iPS cells (Huangfu et al. Nat Biotechnol, 2008). VPA is used to promote the proliferation and self-renewal of human and mouse hematopoietic progenitor cells (Bug et al. Cancer Res, 2005, De Felice et al. Cancer Res, 2005) and suppress differentiation of astrocytes and oligodendrocytes from rat neural progenitor cells (Hsieh et al. Natl Acad Sci USA, 2004, Jung et al. BMC Cell Biol, 2008). Valproic Acid is supplied as a sodium salt of the molecule with ≥ 95% purity; Molecular weight 166.2 g/mol; CAS number 1069-66-5. Visit STEMCELL.com for more information and related products.
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Sigma Aldrich Fine Chemicals Biosciences MITOPQ-5MG
NC2878690 MITOPQ-5MG
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Invivogen H-151 STING INHIBITOR 10MG
Synthetic Indole Derivative - STING Inhibitor - InvitroFit
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Apexbio Technology LLC TAK-285 871026-44-7 10mg
TAK-285 (CAS 871026-44-7) is a small molecule inhibitor targeting the receptor tyrosine kinases HER2 and EGFR with reported IC50 values of 17 nM and 23 nM respectively Both HER2 and EGFR are members of the ErbB receptor family frequently implicated in tumorigenesis through overexpression in various cancers TAK-285 demonstrates selective inhibition of cancer cell lines overexpressing HER2 or EGFR while sparing cells with normal expression levels In xenograft models TAK-285 administration significantly reduced tumor growth Additionally the compound inhibits downstream signaling by suppressing AKT and MAPK phosphorylation TAK-285 serves as a valuable tool for investigating HER2/EGFR-driven oncogenic mechanisms and for evaluating therapeutic strategies targeting these pathways
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Cayman Chemical Fluindione, Purity: ≥98%, CAS: 957-56-2, 10 mg
A vitamin K antagonist; inhibits VKOR (IC50 = 6.6 nM), including VKOR containing certain substitution mutations; inhibits platelet and fibrin deposition, as well as prevents β-thromboglobulin release and thrombin-antithrombin complex formation, in an ex vivo model of tissue factor-induced thrombus formation using isolated human whole blood
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Medchemexpress LLC Recombinant mouse ST6GAL1 protein (HEK293, His-tag) | >95.0% | 5 UG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Recombinant mouse ST6GAL1 protein expressed in HEK293 cells with an N-terminal His tag. The protein (residues K27-C403) is supplied as a filtered, buffered solution and is characterized for purity and enzymatic activity to support biochemical assays and glycosylation studies.
- Recombinant mouse ST6GAL1 expressed in HEK293 cells.
- N-terminal His tag for purification and detection.
- Residues K27-C403 representing the catalytic domain.
- Purity greater than 95% as determined by reducing SDS-PAGE.
- Specific activity greater than 150 pmol/min/μg.
- Supplied in 20 mM Tris, 120 mM NaCl, pH 7.5, 0.22 μm filtered.
- Store at -80°C for long-term storage; avoid repeated freeze-thaw cycles.
- Molecular weight approximately 50-55 kDa.
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Cayman Chemical Pindolol, Purity: ≥99%, CAS: 13523-86-9, 500 mg
A β1- and β2-AR antagonist (Kis = 2.6 and 4.8 nM, respectively); partial agonist of the β3-AR; antagonist of the 5-HT1A receptor (Ki = 81.1 nM for inhibition of 5-HT-stimulated GTPγS binding); inhibits isoproterenol-induced tachycardia in anesthetized cats (ED50 = 1.8 µg/kg); decreases mean blood pressure in conscious spontaneously hypertensive rats at 30 mg/kg per day
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TARGETMOL CHEMICALS INC BLU9931 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. BLU9931 is the first selective small molecule inhibitor of FGFR4. purity: 99%
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Cayman Chemical SJB2-043, Purity: ≥98%, CAS: 63388-44-3, 25 mg
An inhibitor of the USP1-UAF complex (IC50 = 0.544 µM for its deubiquitinase activity) and SARS-CoV-2 PLpro (IC50s = 0.56 and 0.091 µM using Z-LRGG-AMC or Ub-AMC, respectively, as PLpro substrates); reduces the levels of USP1, ID-1, ID-2, and ID-3 in K562 cells at 0.5-10 µM; decreases the viability of K562 cells (EC50 = 1.07 µM); induces apoptosis in K562 cells in a concentration-dependent manner
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